Lead Medical Monitor, Clinical Development, Solid Tumors position at BeOne Medicines.| United States Of America

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BeOne Medicines Lead Medical Monitor, Clinical Development, Solid Tumors

Experience: General

Pattern: Remote

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Remote (US)....United States Of America

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BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. The Director, Clinical Development will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. As a leader in the organization, the incumbent will be accountable to jointly develop clinical program strategy and help assure that activities are executed within expected scope, budget and timelines. The incumbent will play a key role the establishment and growth of Clinical Research functions to assure best-in-class global capabilities and execution. Specifically, the incumbent will work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research. Essential Functions of the Job: Facilitate generation of, author, update, and/or review key documents, including, but not limited to: Protocol concepts, synopses, protocols, and amendments or Informed consent documents; Investigator Brochures or Clinical study reports; Abstracts, posters and manuscripts or Clinical sections of INDs (and equivalent applications), NDAs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports; Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports; Risks / benefits analysis for applicable documents; May contribute to Clinical Development Plans. Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies. Provide scientific expertise for selection of investigator and vendors. Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol. Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO’s. Review, query, and analyze clinical trial data. Interpret, and present clinical trial data both internally and externally. May represent a clinical study or development program on one or more teams or sub teams. Create clinical study or program-related slide decks for internal and external use. Build and maintain opinion leader/investigator networks; organize and present at key opinion leader advisory boards and investigator meetings. Contribute to or perform therapeutic area/indication research and competitor analysis. Build strong relationships with internal experts. Identify continuous process improvement opportunities. Identify incremental organizational resource needs – staff, budget, and systems. Develop, track, execute and report on goals and objectives. Support budget planning and management. Be accountable for compliant business practices. Required Education and Experience: 5 plus years of experience and success within other biotech/pharmaceutical companies. MD, DO or international equivalent degree Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical development role. Clinical oncology experience: candidates with exceptional experience in other therapeutic areas would be considered if they demonstrated clear potential to apply their existing skills to oncology. Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing. High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills. Knowledge of GCP and ICH Guidelines. Flexibility to work with colleagues in a global setting. Able to engage in work-related travel approximately 25%. Strategic leader with demonstrated success building, managing and developing individuals and teams is preferred. Experience with the development and support of related SOPs and policies is expected. Knowledge of industry standard Clinical Development IT solutions expected. Capabilities: Ability to manage multiple projects in a fast-paced environment. Values based collaborator – respectful, accountable and collaborative. Ability to relate and work with a wide range of people to achieve results. Impactful written and verbal scientific communication. Successful and superior influencing skills across all levels of the organization and external collaborators. Problem solving and risk-mitigation skills. Confident, positive attitude. Appreciation of diversity and multiculturalism. Strategic and creative thinker. Ability to build working relations throughout the organization and with business partners to achieve business goals. Strong time management and organizational skills. Skilled in multiple computer-based tools, in addition to software programs such as Word, Project, PowerPoint, Excel, etc. Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity Salary Range: $249,800.00 - $309,800.00 annually BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com .

Lead Medical Monitor, Clinical Development, Solid Tumors job opportunity at BeOne Medicines.

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